Controlled Drug Release from Pharmaceutical Nanocarriers.

Controlled Drug Release from Pharmaceutical Nanocarriers.
复制标题

DOI:
10.1016/j.ces.2014.08.046
复制
发表时间:
2015-03-24
影响因子:
4.7
通讯作者:
Yeo Y
Yeo Y
中科院分区:
工程技术2区
文献类型:
--
作者:
Lee JH;Yeo Y

文献摘要

参考文献

被引文献

相似文献

提供药物释放时空控制的纳米载体有助于降低毒性并提高药物的治疗效果。另一方面,由于纳米载体表面积/体积比大且扩散距离短,因此在控制药物释放动力学方面面临着独特的挑战。为了开发具有理想释放动力学的目标应用纳米载体,重要的是要了解载体保留和释放药物的机制、载体的组成和形态对药物释放动力学的影响以及纳米载体的制备和修饰的现有技术。本综述概述了药物释放机制和各种纳米载体,特别强调控制药物释放动力学的方法。
Nanocarriers providing spatiotemporal control of drug release contribute to reducing toxicity and improving therapeutic efficacy of a drug. On the other hand, nanocarriers face unique challenges in controlling drug release kinetics, due to the large surface area per volume ratio and the short diffusion distance. To develop nanocarriers with desirable release kinetics for target applications, it is important to understand the mechanisms by which a carrier retains and releases a drug, the effects of composition and morphology of the carrier on the drug release kinetics, and current techniques for preparation and modification of nanocarriers. This review provides an overview of drug release mechanisms and various nanocarriers with a specific emphasis on approaches to control the drug release kinetics.
用于全身性抗癌药物和siRNA的全层纳米颗粒,用于潜在的三阴性乳腺癌治疗。
DOI: 10.1021/nn4047925
发表时间: 2013-11-26
期刊: ACS NANO
影响因子: 17.1
作者:
Deng, Zhou J.;Morton, Stephen W.;Ben-Akiva, Elana;Dreaden, Erik C.;Shopsowitz, Kevin E.;Hammond, Paula T.
通讯作者: Hammond, Paula T.
DOI: 10.1016/s0168-3659(02)00212-2
发表时间: 2002-10-04
影响因子: 10.8
作者:
Fonseca, C;Simoes, S;Gaspar, R
通讯作者: Gaspar, R
DOI: 10.1016/j.ijpharm.2011.08.038
发表时间: 2011-11-28
影响因子: 5.8
作者:
Chang, Cong;Wei, Hua;Zhuo, Ren-Xi
通讯作者: Zhuo, Ren-Xi
DOI: 10.1016/s0378-5173(03)00132-7
发表时间: 2003-05-12
影响因子: 5.8
作者:
Bhadra, D;Bhadra, S;Jain, NK
通讯作者: Jain, NK
DOI: 10.1021/la302433a
发表时间: 2012-08-07
期刊: LANGMUIR
影响因子: 3.9
作者:
Cao, Zhiqiang;Zhang, Lei;Jiang, Shaoyi
通讯作者: Jiang, Shaoyi